Event Group
Event Groups are part of the Adverse Events Module within the Results Section. They provide a way to organize and summarize adverse event data by grouping related events together.
Each Event Group typically represents a category or class of adverse events and includes statistical information such as the number of participants affected and at risk for different event types: deaths, serious events, and other events.
Event Group path is as follows:
Study -> Results Section -> Adverse Events Module -> Event Group
Event Group
Ignite Creation Date:
2025-12-25 @ 2:01 AM
Ignite Modification Date:
2025-12-26 @ 12:25 AM
NCT ID:
NCT02312960
Group ID:
EG001
Title:
From Study 15396 Placebo+Abi/Pred Group
Description:
Safety FU from feeder study 15396. Participants received placebo matched to radium-223 dichloride at intervals of every 4 weeks, along with abiraterone acetate plus prednisone/prednisolone (abi/pred) for up to 6 cycles.
Deaths Number Affected:
32
Deaths Number At Risk:
None
Serious Number Affected:
4
Serious Number At Risk:
49
Other Number Affected:
6
Other Number At Risk:
49
Study:
NCT02312960
Results Section:
NCT02312960
Adverse Events Module:
NCT02312960